The Recall Desk

Manufacturer

Teleflex Medical

204 recalls in our database name Teleflex Medical as the manufacturing or recalling firm.

What the numbers show

Total
204
Critical
9
Severe
8
Most recent
2020-01-22

Of the 204 recalls from Teleflex Medical we have scored against our rubric, 9 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 8 (4%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

201–204 of 204

  • ModerateFDA (Devices)·Z-1158-2013·2013-05-01

    Teleflex Medical Recalls Belly Bag Urine Collection Bags Due to Packaging Concerns

    Teleflex Medical is recalling 190,103 sterile Belly Bag Urine Collection Bags with Hip Belts because the sterile packaging may be compromised.

    Product
    Belly Bag Urine Collection Bag with Hip Belt. The product is a sterile urine collection device that collects urine by mechanical means when attached to an indwelling Foley or suprapubic catheter.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0078-2013·2012-10-24

    Teleflex Recalls Hem-o-lok Polymer Clips Due to Sterility Concerns

    Teleflex Medical is recalling 126 units of Hem-o-lok Large Polymer Ligating Clips because pinholes in the trays may compromise sterility.

    Product
    Hem-o-lok Large Polymer Ligating Clips, REF #544240, Rx only, Sterile, Teleflex Medical, Research Triangle Park, NC 27709. Teleflex Medicals Hem-o-lok polymer ligating clips are single use, sterile, non-absorbable medial devices that have been designed to ligate vessels and t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2186-2012·2012-08-22

    Teleflex Medical Recalls TAUT Cholangiogram Catheter Intraducer Due to Missing Label

    Teleflex Medical is recalling 611 units of TAUT Cholangiogram Catheter Intraducers because the internal packaging is missing labels. The devices were distributed to 27 states.

    Product
    TAUT, Cholangiogram Catheter Intraducer, Peritoneal Catheter, Teleflex Medical, Research Triangle Park, NC. An introduction/drainage catheter accessory is intended to aid in the manipulation of or insertion of the device into the body.
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-2036-2012·2012-07-25

    Teleflex Medical Recalls Hudson RCI Concha Therm Neptune Humidifiers

    Teleflex Medical is recalling Hudson RCI Concha Therm Neptune Humidifiers because a speaker failure could prevent audio alarms from sounding, potentially delaying patient treatment.

    Product
    Hudson RCI Concha Therm Neptune Humidifier, Rx Only, Product Usage: Usage: Device that is intended to add moisture to, and sometime to warm, the breathing gases for administration to a patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

Teleflex Medical

Czech company

Country
Czech Republic

Source: Wikidata (Q121622528), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.